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The Ocean Co Ltd

FDA import alert and refusal historyIncheon, South KoreaFEI 3009807821

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Example subjectThe Ocean Co Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, The Ocean Co Ltd (Incheon, South Korea) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for flounder (live or processed); turbot (live or processed), published by FDA on December 22, 2017, and has 8 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Turbot · MFRHACCP
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for The Ocean Co Ltd

11 records, newest first. Each line links to the FDA page it came from.

2020

  1. Import refusal
    Refused, TurbotMFRHACCPEntry 9AR-0321892-2
    Source
  2. Import refusal
    Refused, Aquaculture harvested fishery/seafood products, n.e.c.,MFRHACCPEntry EVJ-0259667-7
    Source
  3. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2019

  1. Import refusal
    Refused, 3 lines in one entry: Flounder (arrowtooth, dab, fluke)NO PROCESSEntry AFF-2011484-9Show 3 lines
    Source
  2. Import refusal
    Refused, 3 lines in one entry: Flounder (arrowtooth, dab, fluke)MFRHACCPEntry AFF-2011471-6Show 3 lines
    • Refused, Flounder (arrowtooth, dab, fluke)MFRHACCPEntry AFF-2011471-6Source
    • Refused, Flounder (arrowtooth, dab, fluke)MFRHACCPEntry AFF-2011471-6Source
    • Refused, Flounder (arrowtooth, dab, fluke)MFRHACCPEntry AFF-2011471-6Source
    Source

2017

  1. Import alert listing
    Listed on Import Alert 16-120red listFlounder (live or processed); Turbot (live or processed)
    Source
  2. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • MFRHACCP5 refused lines

    Seafood HACCP requirements not met

    The seafood appeared to have been processed without meeting the seafood HACCP requirements in 21 CFR 123.6(a) and 123.8(a), so it is treated as prepared under insanitary conditions.

  • NO PROCESS3 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about The Ocean Co Ltd

Is The Ocean Co Ltd on an FDA import alert?
Yes. As of October 26, 2026, The Ocean Co Ltd is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for flounder (live or processed); turbot (live or processed); FDA published the listing on December 22, 2017.
Has FDA refused shipments from The Ocean Co Ltd?
Yes. FDA refused 8 shipment lines from The Ocean Co Ltd between December 19, 2019 and August 4, 2020. The most recent, on August 4, 2020, was turbot, charged as MFRHACCP (seafood haccp requirements not met).
Why did FDA refuse The Ocean Co Ltd's shipments?
The most frequent charges are MFRHACCP (seafood haccp requirements not met, 5 lines) and NO PROCESS (no scheduled process filed, 3 lines).
When was The Ocean Co Ltd last inspected by FDA?
FDA's most recent inspection of The Ocean Co Ltd with a final classification is dated February 14, 2020 and was classified VAI (Voluntary Action Indicated).
What is The Ocean Co Ltd's FEI number?
The Ocean Co Ltd's FDA Establishment Identifier (FEI) is 3009807821.
Can shipments from The Ocean Co Ltd still enter the U.S.?
Shipments of flounder (live or processed); turbot (live or processed) from The Ocean Co Ltd can be detained without physical examination under Import Alert 16-120; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectThe Ocean Co Lt added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.